Citation: Peng Wei, Qi Peiyao, Dong Kaixuan, He Aihua. Oligomerization and Polymerization of Isoprene Catalyzed by Alkylaluminium with Different Structures[J]. Acta Chimica Sinica, ;2020, 78(12): 1418-1425. doi: 10.6023/A20070336 shu

Oligomerization and Polymerization of Isoprene Catalyzed by Alkylaluminium with Different Structures

Shandong Provincial Key Laboratory of Olefin Catalysis and Polymerization, Key Laboratory of Rubber-Plastics (Ministry of Education), School of Polymer Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042, China
Shandong Provincial Key Laboratory of Olefin Catalysis and Polymerization, Key Laboratory of Rubber-Plastics (Ministry of Education), School of Polymer Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042, China

Corresponding author: He Aihua, ahhe@qust.edu.cn; aihuahe@iccas.ac.cn
Received Date: 30 July 2020
Available Online: 9 October 2020
Fund Project: Project supported by the Major Scientific and Technological lnnovation Project of Shandong Province(No.2019JZZY010352) and Taishan Scholar Programthe Major Scientific and Technological lnnovation Project of Shandong Province 2019JZZY010352

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Alkylaluminium (AlR₃), as co-catalyst component in Ziegler-Natta catalytic system, plays important roles in the alkylation, forming and changing the structure and concentration of active centers through the reduction and reversible adsorption-desorption reactions with the metal compound of the catalyst, acting as chain transfer agent, etc. However, the alkylaluminium itself do have the catalytic effect on the conjugated diene monomers. In this article, alkylaluminium with different structures such as triethylaluminium (AlEt₃), triisobutylaluminium (Al(i-Bu)₃), diisobutylaluminium hydride (AlH(i-Bu)₂), diethylaluminium chloride (AlEt₂Cl), ethylaluminium dichloride (AlEtCl₂) were used to catalyze isoprene oligomerization and polymerization. The effects of the structure and concentration of alkylaluminiums (n(Al)/n(M)=7×10^-5, 35×10^-5, 350×10^-5, 1050×10^-5) on the catalytic behaviors of isoprene were studied. The microstructure (trans-1, 4 and cis-1, 4), molecular weight and molecular weight distribution of the products were characterized by ¹H nuclear magnetic resonance spectroscopy (¹H NMR), gel permeation chromatography (GPC) and gas chromatography-mass spectrometry (GC-MS). It was found that alkylaluminium could initiate oligomerization and cationic polymerization of isoprene under the minor incorporation of H₂O, which were affected greatly by the structure and concentration of alkylaluminium. Using AlEtCl₂ led to the highest catalytic activity and produced products containing more linear polymers with mixed cis-1, 4/trans-1, 4 structures when n(Al)/n(M)=1050×10^-5. The Al(i-Bu)₃ and AlH(i-Bu)₂ didn't have basically cation initiation ability, which led to isoprene oligomerization. The alkylaluminium with n(Al)/n(M) ≤ 350×10^-5 had negligible influence on the isoprene polymerization and oligomerization. And lower or higher alkylaluminium concentration were not beneficial to obtain polyisoprene with high molecular weight. The catalytic mechanism of alkylaluminium on isoprene was discussed, which provided a further understanding on the catalytic behavior of alkylaluminium components in Ziegler-Natta catalyst and the effect of alkylaluminium on polymers.
- alkylaluminium,
- isoprene,
- catalysis,
- oligomerization,
- polymerization behavior
1. [1]
  Mori, H.; Hasebe, K.; Terano, M. Polymer 1999, 40, 1389.
2. [2]
  Yang, H. R.; Zhang, L. T.; Zang, D. D.; Fu, Z. S.; Fan, Z. Q. Catal. Commun. 2015, 62, 104.
3. [3]
  Bahri-Laleh, N.; Correa, A.; Mehdipour-Ataei, S.; Arabi, H.; Haghighi, M. N.; Zohuri, G.; Cavallo, L. Macromolecules 2011, 44, 778.
4. [4]
  Liu, B. P.; Nitta, T.; Nakatani, H.; Terano, M. Macromol. Chem. Phys. 2002, 203, 2412.
5. [5]
  Liu, B. P.; Nitta, T.; Nakatani, H.; Terano, M. Macromol. Chem. Phys. 2003, 204, 395.
6. [6]
  Liu, B. P.; Nitta, T.; Nakatani, H.; Terano, M. Macromol. Symp. 2004, 213, 7.
7. [7]
  Potapov, A. G.; Terskikh, V. V.; Zakharov, V. A.; Bukatov, G. D. J. Mol. Catal. A:Chem. 1999, 145, 147.
8. [8]
  Potapov, A. G.; Terskikh, V. V.; Bukatov, G. D.; Zakharov, V. A. J. Mol. Catal. A:Chem. 2000, 158, 457.
9. [9]
  Hu, J.; Han, B.; Shen, X. R.; Fu, Z. S.; Fan, Z. Q. Chin. J. Polym. Sci. 2013, 31, 583.
10. [10]
  Franceschini, F. C.; Tavares, T. T. D. R.; Greco, P. P.; Galland, G. B.; dos Santos, J. H.; Soares, J. B. J. Appl. Polym. Sci. 2005, 95, 1050.
11. [11]
  Rocha, T. C. J.; Coutinho, F. M. B.; Soares, B. G. Polym. Bull. 2009, 62, 1.
12. [12]
  Gao, H.; Liu, X.; Tang, Y.; Pan, J.; Wu, Q. Polym. Chem. 2011, 2, 1398.
13. [13]
  Huang, W. Q.; Yang, L.; Zhao, X.; Man, Y.; Li, B. Y.; Zhang, Y.; Yang, W. T. Chem. Ind. & Eng. Pro. 2011, 30, 1231(in Chinese).
14. [14]
  Blaakmeer, E. S. M.; van Eck, E. R. H.; Kentgens, A. P. M. Phys. Chem. Chem. Phys. 2018, 20, 7974.
15. [15]
  Niu, Q. T.; Zhang, J. Y.; Peng, W.; Fan, Z. Q.; He, A. H. Mol. Catal. 2019, 471, 1.
16. [16]
  Richardson, W. S. J. Polym. Sci. 1954, 13, 325.
17. [17]
  Ferington, T. E.; Tobolsky, A. V. J. Polym. Sci. 1958, 31, 25.
18. [18]
  Dolgoplosk, B.; Belonovskaia, G. P.; Boldyreva, I. I.; Nelson, K. V.; Kropacheva, E. N.; Rosinoer, J. M.; Chernova, J. D. J. Polym. Sci. 1961, 53, 209.
19. [19]
  Kennedy, J. P.; Squires, R. G. Polymer 1965, 6, 579.
20. [20]
  Binder, J. L. J. Polym. Sci. Part A:Gen. Pap. 1963, 1, 37.
21. [21]
  Kössler, I.; Vodehnal, J.; Štolka, M. J. Polym. Sci. Part A:Gen. Pap. 1965, 3, 2081.
22. [22]
  Pétiaud, R.; Taärit, Y. B. J. Chem. Soc. 1980, 10, 1385.
23. [23]
  Peng, Y. X.; Deng, Y. G.; Liu, J. L.; Dai, H. S.; Cun, L. F. Polym. Mater. Sci. Eng. 1997, 13, 95(in Chinese).
24. [24]
  Gaylord, N. G.; Matyska, B.; Mach, K.; Vodehnal, J. J. Polym. Sci. Pol. Chem. 1966, 4, 2493.
25. [25]
  Gaylord, N. G.; Kössler, I.; Matyska, B.; Mach, K. J. Polym. Sci. Pol. Chem. 1968, 6, 125.
26. [26]
  Matyska, B.; Doležal, I.; Kössler, I. Collect. Czech. Chem. C 1971, 36, 2924.
27. [27]
  Uchida, Y.; Furuhata, K. I.; Ishiwata, H. Bull. Chem. Soc. Jpn. 1971, 44, 1118.
28. [28]
  Akutagawa, S.; Taketomi, T.; Otsuka, S. Chem. Lett. 1976, 5, 485.
29. [29]
  Shen, G. L. Journal of Liaoyang Petrochemical College 1996, 12, 1(in Chinese).
30. [30]
  Yu, S. J. Speciality Petrochemicals 2000, (2), 20(in Chinese).
31. [31]
  Shen, G. L.; Tang, L. H. Speciality Petrochemicals 2004, (1), 17(in Chinese).
32. [32]
  Xia, S. W.; Xia, S. W.; Ma, S. X. Acta Polym. Sinica 1998, (3), 262(in Chinese).
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